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https://elar.urfu.ru/handle/10995/90046
Title: | Synthesis of Heteroannulated Indolopyrazines through Domino N-H Palladium-Catalyzed/Metal-Free Oxidative C-H Bond Activation |
Authors: | Kvashnin, Y. A. Verbitskiy, E. V. Zhilina, E. F. Rusinov, G. L. Chupakhin, O. N. Charushin, V. N. |
Issue Date: | 2020 |
Publisher: | American Chemical Society |
Citation: | Synthesis of Heteroannulated Indolopyrazines through Domino N-H Palladium-Catalyzed/Metal-Free Oxidative C-H Bond Activation / Y. A. Kvashnin, E. V. Verbitskiy, E. F. Zhilina, G. L. Rusinov, et al. . — DOI 10.1021/acsomega.0c01945 // ACS Omega. — 2020. — Vol. 25. — Iss. 5. — P. 15681-15690. |
Abstract: | A convenient approach to [1,2,5]oxadiazolo[3′,4′:5,6]pyrazino[2,3-b]indoles and their heteroannulated analogues bearing various aryl substituents in the backbone has been developed. This synthetic protocol is based on Pd-catalyzed Buchwald-Hartwig and subsequent annulation by intramolecular oxidative cyclodehydrogenation. The photophysical properties for new polycycles have been measured. © 2020 American Chemical Society. |
URI: | http://elar.urfu.ru/handle/10995/90046 |
Access: | info:eu-repo/semantics/openAccess |
SCOPUS ID: | 85087745933 |
WOS ID: | 000546100300086 |
PURE ID: | 13401406 |
ISSN: | 2470-1343 |
DOI: | 10.1021/acsomega.0c01945 |
Sponsorship: | Russian Foundation for Basic Research, RFBR: 18-29-23045, 18-33-00103-mol_a This work was supported by the Russian Foundation for Basic Research (research project no. 18-29-23045 mk). Y.A.K. would like to acknowledge the financial support for the part of the synthetic section from the Russian Foundation for Basic Research (research project no. 18-33-00103-mol_a). |
Appears in Collections: | Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC |
Files in This Item:
File | Description | Size | Format | |
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10.1021-acsomega.0c01945.pdf | 1,41 MB | Adobe PDF | View/Open |
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